Oncology Clinical Research Coordinator II — Part-Time

3455 Illingworth Research Group (Spain) Sociedad Limitada; Barcelona; Híbrido; EUR 24.000 - 42.000; A tiempo parcial

Descripción de la vacante

Illingworth Research Group is seeking a Clinical Research Coordinator II for sabadell or Barcelona area with oncology experience. The role involves planning and preparing protocols, maintaining TMF, coordinating startup activities, and supporting the PI with daily study tasks. The candidate will recruit and screen participants, ensure GCP compliance, and assist with audits. Flexible scheduling and cross-site collaboration are expected.

Formación

• Registered Nurse or university degree (BS) in a relevant field.
• Minimum 1 year of clinical research experience, coordination preferred.
• Knowledge of regulations, ICH-GCP, privacy and guidelines.
• Strong problem solving, planning and evaluation skills.
• Ability to manage multiple tasks and meet deadlines.
• Good interpersonal and communication skills within a team.

Responsabilidades

• Plan and prepare clinical research projects and timelines.
• Maintain Investigator Site File/TMF and regulatory documents.
• Coordinate startup activities, clinic logistics and staff training.
• Support PI with daily tasks, visit calendars, and monitor visits.
• Recruit, screen, and consent potential study participants.
• Ensure study activities comply with protocol, SOPs and regulations.
• Coordinate routine data entry and report adverse events.
• Assist with audits and sponsor/QA visits.
• Provide status updates to project managers and sponsors.
• Maintain TMF and close-out documentation.

Conocimientos

Problem solving

Planning

Evaluation

Time management

Attention to detail

Interpersonal skills

Multi-tasking

SOP writing

Educación

Registered Nurse

Bachelor of Science

Herramientas

Word

Excel

PowerPoint

EDC software

Descripción del empleo

Illingworth Research Group is seeking a Clinical Research Coordinator II for sabadell or Barcelona area with oncology experience. The role involves planning and preparing protocols, maintaining TMF, coordinating startup activities, and supporting the PI with daily study tasks. The candidate will recruit and screen participants, ensure GCP compliance, and assist with audits. Flexible scheduling and cross-site collaboration are expected.